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Contribution of cardiac muscle cell disorganization to the clinical features of hypertrophic cardiomyopathy
Authors:S. Morimoto  Morie Sekiguchi  Shinya Hiramitsu  Akihisa Uemura  Toshio Nishikawa  Hitoshi Hishida
Affiliation:(1) Division of Cardiology, Department of Internal Medicine, Fujita Health University School of Medicine, Toyoake 470-1192, Japan Tel. +81-562-93-2312; Fax +81-562-93-2315 e-mail: morimoto@fujita-hu.ac.jp, JP;(2) Department of Pathology, Tokyo Women's Medical University, Tokyo, Japan, JP
Abstract:Heart failure rarely develops in the setting of hypertrophic cardiomyopathy (HCM). Because of this, cardiac muscle cell disorganization (CD), which is a histologic characteristic of HCM, is not believed to be responsible for the development of systolic dysfunction. The aim of the present study was to clarify whether CD can cause systolic dysfunction and ventricular dilation in patients with HCM. Sixteen hearts from patients with HCM obtained at autopsy were divided into two groups: group A (n = 11), without biventricular dilation, and group B (n = 5), with dilation. Specimens consisting of transverse and longitudinal tissue sections of the ventricles were prepared, and the extent of CD and interstitial fibrosis was quantified, using light microscopy. None of the patients in group A had had chronic congestive heart failure, while all of the patients in group B had died of congestive heart failure. In group B, CD was not limited to the interventricular septum. Rather, diffuse CD was observed in both ventricular free walls. The extent of CD was significantly greater in group B than in group A, while the degree of interstitial fibrosis was similar in the two groups (13.6% in group A vs 14.6% in group B). These results suggest that CD may be responsible for systolic dysfunction and ventricular dilation. Received: July 11, 2000 / Accepted: November 25, 2000
Keywords:Hypertrophic cardiomyopathy  Cardiac muscle cell disorganization  Congestive heart failure
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